Z-2707-2016 Class II Terminated

Recalled by Limacorporate S.p.A — San Daniele Del Friuli, N/A

FDA device recall Z-2707-2016 was initiated by Limacorporate S.p.A on July 21, 2016 and is designated Class II. Reason for recall: Product found to be dimensionally non-conforming (slightly over dimensioned on the diameter of the Zimmer connection) and non-functional for connecting with some T-handles. The recall status is terminated (terminated January 13, 2017). Affected quantity: 76.

Recall Details

Product Type
Devices
Report Date
September 7, 2016
Initiation Date
July 21, 2016
Termination Date
January 13, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
76

Product Description

SMR allen wrench 5 mm, product code 9013.50.210

Reason for Recall

Product found to be dimensionally non-conforming (slightly over dimensioned on the diameter of the Zimmer connection) and non-functional for connecting with some T-handles.

Distribution Pattern

US, Italy, Australia

Code Information

14AA311